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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
THRB
(R320C +1 more)
Single nucleotide variant
(missense variant)
THRB-related disorder
+4 more
GPathogenic
LOC126806630, THRB
(R243Q +1 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GPathogenic
THRB
(I28V +1 more)
Single nucleotide variant
(missense variant)
Selective pituitary resistance to thyroid hormone
+4 more
GBenign/Likely benign
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